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  4. NDC Product Code: 71589-019 Docosanol

NDC 71589-019 Docosanol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71589-019?
  5. Docosanol Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71589-019
Proprietary Name:
Docosanol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aleor Dermaceuticals Limited
Labeler Code:
71589
Product Label ID:
952520e5-dfc9-4946-941c-08560ce3d957
Start Marketing Date: [9]
05-03-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 71589-019-01

Package Description: 1 TUBE in 1 PACKAGE / 2 g in 1 TUBE

NDC Code 71589-019-03

Package Description: 1 BOTTLE, PUMP in 1 PACKAGE / 2 g in 1 BOTTLE, PUMP

Product Details

What is NDC 71589-019?

The NDC code 71589-019 is assigned by the FDA to the product Docosanol which is product labeled by Aleor Dermaceuticals Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71589-019-01 1 tube in 1 package / 2 g in 1 tube, 71589-019-03 1 bottle, pump in 1 package / 2 g in 1 bottle, pump. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Docosanol?

Adults and children 12 years or over: wash hands before and after applying creamapply to affected area on the face or lips at the first sign of cold sore/fever blister (tingle).early treatment ensures the best resultsrub in gently but completelyuse 5 times a day until healedchildren under 12 years: ask a doctor

Which are Docosanol UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Docosanol Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Docosanol?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".